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Human Papillomavirus Combination

NDC 63083-4019 · Professional Complementary Health Formulas

Generic nameHuman Papillomavirus Combination
Dosage formLIQUID
RouteORAL
Active ingredient(s)HUMAN ADENOVIRUS B SEROTYPE 3, MUSA ACUMINATA WHOLE, HUMAN PAPILLOMAVIRUS SEROTYPE 16 WHOLE
Strength12; 30; 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Marketing categoryUNAPPROVED HOMEOPATHIC

Packages

63083-4019-2 — 59 mL in 1 BOTTLE, DROPPER (63083-4019-2)

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels